Infection process and sloughing off of rhizobial outer membrane in effective nodules of lima bean

1982 ◽  
Vol 28 (7) ◽  
pp. 890-896 ◽  
Author(s):  
Arya K. Bal ◽  
Peter P. Wong

In addition to infection via root hairs, infection threads originating in epidermal cells after colonization of epidermis have been clearly demonstrated in lima beans infected with Rhizobium sp. 127E15, and this double mode of infection possibly accounts for profuse nodulation of the roots. Sloughing off of the outer membrane (cell wall) was detected after release of rhizobia during bacteroid differentiation in effective nodules.

1986 ◽  
Vol 64 (10) ◽  
pp. 2216-2226 ◽  
Author(s):  
Yves Prin ◽  
Mireille Rougier

The aim of the present study was to investigate the Alnus root surface using seedlings grown axenically. This study has focused on root zones where infection by the symbiotic actinomycete Frankia takes place. The zones examined extend from the root cap to the emerging root hair zone. The root cap ensheaths the Alnus root apex and extends over the root surface as a layer of highly flattened cells closely appressed to the root epidermal cell wall. These cells contain phenolic compounds as demonstrated by various histochemical tests. They are externally bordered by a thin cell wall coated by a thin mucilage layer. The root cap is ruptured when underlying epidermal cells elongate, and cell remnants are still found in the emerging root hair zone. Young emerging root hairs are bordered externally by a cell wall covered by a thin mucilage layer which reacts positively to the tests used for the detection of polysaccharides, glycoproteins, and anionic sites. The characteristics of the Alnus root surface and the biological function of mucilage and phenols present at the root surface are discussed in relation to the infection process.


1989 ◽  
Vol 67 (8) ◽  
pp. 2435-2443 ◽  
Author(s):  
M. F. Le Gal ◽  
S. L. A. Hobbs

Pisum sativum L., cv. Afghanistan, does not form nodules with 128C52, a North American strain of Rhizobium leguminosarum. Timing of the abortion of the nodulation process was determined by microscopy in both 'Afghanistan' and nonnodulating 'Trapper,' produced by backcrossing the nonnodulating genes of 'Afghanistan' into 'Trapper,' a North American variety. Three to 5 days after inoculation, we observed deformed roots and localized swellings as well as loosely curled root hairs in these nonnodulating combinations. Rhizobia entered root hairs and epidermal cells, but no infection threads were seen. Cortical cells divided and a nodule meristem was initiated. Some meristematic cells showed abnormal features such as a high concentration of free ribosomes, dilated endoplasmic reticulum often connected to a dilated nuclear envelope, and disrupted mitochondria. Cortical cells around the nodule meristem were devoid of starch grains. Such phenotypes are known to be associated with rhizobial mutants, but in this case a plant effect is responsible.


1983 ◽  
Vol 29 (1) ◽  
pp. 69-76 ◽  
Author(s):  
Steven G. Pueppke

Eight lines of soybean (Glycine max), four of wild soybean (Glycine soja), and one cowpea (Vigna unguiculata) cultivar were inoculated with 18 Rhizobium strains. After 4 days, root hairs were examined for infection threads. Threads were produced by all hosts but exclusively in nodulating combinations. Only Rhizobium sp. strains 3G4b9a and 3G4b19 were inconsistent; they nodulated soybean and G. soja in some experiments, but rarely formed infection threads. Soybean and G. soja were indistinguishable in their interactions with rhizobia, as were lele soybean lines (genetically lack soybean lectin), Hardee soybean (contains the noduation-influencing genes Rj2 and Rj3), and several other soybean cultivars. Threads formed in cowpea with all of the R. japonicum strains and most Rhizobium sp. but not with R. lupini. Infection of all three host species occurred in portions of the primary root containing immature or no root hairs at the time of inoculation; proximal tissues having elongated root hairs lacked infection threads. Infected root hairs were short and commonly shaped like question marks. Threads usually branched and sometimes intertwined prior to elongation into the basal portion of root hairs.


1982 ◽  
Vol 60 (2) ◽  
pp. 152-161 ◽  
Author(s):  
B. Gillian Turgeon ◽  
Wolfgang D. Bauer

The time course of early infection events in Glycine max following inoculation with Rhizobium japonicum is described. Bacteria became attached to epidermal cells and root hairs within minutes of inoculation. Marked root hair curling occurred within 12 h. Infection thread formation was visible at the light microscope level of resolution about 24 h after inoculation. Infections were observed in short, tightly curled root hairs. These root hairs had not yet emerged at the time of inoculation. Infection threads appeared to originate in pockets formed by contact of the cell wall of the curled root hair with itself. Infection threads in the hairs were multiple and (or) branched. By 48 h, the infection thread(s) had progressed to the base of the root hair but had not yet penetrated into the cortex. Increases in cortical cell cytoplasm and in mitotic division occurred in advance of the penetrating infection thread. A nodule meristem developed in the outer cortex next to the infected root hair by 4 days and was accompanied by cell division across the cortex.


1976 ◽  
Vol 54 (14) ◽  
pp. 1633-1636 ◽  
Author(s):  
T. L. Degenhardt ◽  
T. A. Larue ◽  
E. A. Paul

A non-nodulating cultivar of Pisum sativum cv. Afghanistan was studied to characterize the nature and location of the non-nodulating factor. Nodule formation was not temperature sensitive. Rhizobium leguminosarum could exist in the rhizosphere. Root secretions did not decrease nodulation in adjacent normal plants, nor did the proximity of normal plants promote nodulation. Infection threads formed in the root hairs, but nodules were not formed. The infection process apparently aborted, resulting in the formation of swellings on areas of the root where nodulation would normally occur. Grafting experiments indicate that the factor preventing nodulation is in the root and is not translocated from the cotyledon or plant top.


1983 ◽  
Vol 97 (3) ◽  
pp. 787-794 ◽  
Author(s):  
C H Wong ◽  
C E Pankhurst ◽  
A Kondorosi ◽  
W J Broughton

We examined expression of the megaplasmid pRme41b of Rhizobium meliloti in two different Rhizobium sp. Strains and in Agrobacterium tumefaciens. Transfer of pRme41b into these bacteria was facilitated by insertion of a recombinant plasmid coding for mobilization functions of RP4 into the nif region (Kondorosi, A., E. Kondorosi, C.E. Pankhurst, W. J. Broughton, and Z. Banfalvi, 1982, Mol. Gen. Genet., 188:433-439). In all cases, transconjugants formed nodule-like structures on the roots of Medicago sativa. These structures were largely composed of meristematic cells but they were not invaded by bacteria. Bacteria were found only within infection threads in root hairs, and within intercellular spaces of the outermost cells of the structures. The donor strain of R. meliloti containing pAK11 or pAK12 in pRme41b initially produced nodules on M. sativa that did not fix nitrogen (Fix-). In these nodules, bacteria were released from infection threads into the host cells but they did not multiply appreciably. Any bacteroids formed degenerated prematurely. In some cases, however, reversion to a Fix+ phenotype occurred after 4 to 6 wk. Bacteria released into newly infected cells in these nodules showed normal development into bacteriods.


2017 ◽  
Author(s):  
Adam M. Saffer ◽  
Vivian F. Irish

AbstractRhamnose is required in Arabidopsis thaliana for synthesizing pectic polysaccharides and glycosylating flavonols. RHAMNOSE BIOSYNTHESIS1 (RHM1) encodes a UDP-L-rhamnose synthase, and rhm1 mutants exhibit many developmental defects, including short root hairs, hyponastic cotyledons, and left-handed helically twisted petals and roots. It has been proposed that the hyponastic cotyledons observed in rhm1 mutants are a consequence of abnormal flavonol glycosylation, while the root hair defect is flavonol-independent. We have recently shown that the helical twisting of rhm1 petals results from decreased levels of rhamnose-containing cell wall polymers. In this work, we find that flavonols indirectly modify the rhm1 helical petal phenotype by altering rhamnose flux to the cell wall. Given this finding, we further investigated the relationship between flavonols and the cell wall in rhm1 cotyledons. We show that decreased flavonol rhamnosylation is not responsible for the cotyledon phenotype of rhm1 mutants. Instead, flavonols provide a large reservoir of rhamnose, and blocking flavonol synthesis or rhamnosylation can suppress rhm1 defects by diverting rhamnose to the synthesis of cell wall polysaccharides. Therefore, rhamnose is required in the cell wall for normal expansion of cotyledon epidermal cells. Our findings suggest a broad role for rhamnose-containing cell wall polysaccharides in the morphogenesis of epidermal cells.


1987 ◽  
Vol 65 (3) ◽  
pp. 553-558 ◽  
Author(s):  
Sergio M. de Faria ◽  
Shona G. McInroy ◽  
Janet I. Sprent

A survey of the structure of nodules from primitive legume trees was conducted. All genera examined in the subfamily Caesalpinioideae, some from the Papilionoideae, but none from the Mimosoideae had cells in the central, nitrogen-fixing region in which bacteria were confined by host cell wall material in structures resembling infection threads. However, infection of these cells occurred by intercellular spread of rhizobia rather than by infection threads. It is suggested that infection threads may have evolved in infected cells and later extended to early stages of the infection process including entry into root hairs.


2011 ◽  
Vol 24 (7) ◽  
pp. 798-807 ◽  
Author(s):  
Marta Robledo ◽  
José I. Jiménez-Zurdo ◽  
M. José Soto ◽  
Encarnación Velázquez ◽  
Frank Dazzo ◽  
...  

The establishment of rhizobia as nitrogen-fixing endosymbionts within legume root nodules requires the disruption of the plant cell wall to breach the host barrier at strategic infection sites in the root hair tip and at points of bacterial release from infection threads (IT) within the root cortex. We previously found that Rhizobium leguminosarum bv. trifolii uses its chromosomally encoded CelC2 cellulase to erode the noncrystalline wall at the apex of root hairs, thereby creating the primary portal of its entry into white clover roots. Here, we show that a recombinant derivative of R. leguminosarum bv. trifolii ANU843 that constitutively overproduces the CelC2 enzyme has increased competitiveness in occupying aberrant nodule-like root structures on clover that are inefficient in nitrogen fixation. This aberrant symbiotic phenotype involves an extensive uncontrolled degradation of the host cell walls restricted to the expected infection sites at tips of deformed root hairs and significantly enlarged infection droplets at termini of wider IT within the nodule infection zone. Furthermore, signs of elevated plant host defense as indicated by reactive oxygen species production in root tissues were more evident during infection by the recombinant strain than its wild-type parent. Our data further support the role of the rhizobial CelC2 cell wall–degrading enzyme in primary infection, and show evidence of its importance in secondary symbiotic infection and tight regulation of its production to establish an effective nitrogen-fixing root nodule symbiosis.


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